# DONEPEZIL HYDROCHLORIDE

NDC: 68180-527
Generic name: DONEPEZIL HYDROCHLORIDE
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20151221

FDA application: ANDA202782

## Active ingredients

- DONEPEZIL HYDROCHLORIDE: 23 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-527"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-527
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=03e26183-3e07-45e8-a414-a8bad32483e2